K073090

Substantially Equivalent

RECOVERY G2 FILTER SYSTEM - FEMORAL DELIVERY KIT, MODEL RF-310F; JUGULAR/SUBCLAVAIN DELIVERY KIT, MODEL RF-320J

Applicant: C.R. Bard, Inc.
Product code: DTK
Advisory panel: Cardiovascular
Date received: 2007-11-01
Decision date: 2008-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tempe, AZ, US

Adverse events under product code DTK

product code DTK

Death: 208
Injury: 11,286
Malfunction: 3,002
Total: 14,496

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.